Luminescent organisms have been widely used to develop toxicity tests. However, bioluminescence-based methods are often nonspecific and unsuitable for storage. In this study, the marine luminescent bacterium Vibrio fischeri was grown in various media. After immobilization on insoluble fibroin film (IFF)-coated tubes, the luminescence intensity was measured. Late-log cultures grown in nutrient broth containing 3 or 5% NaCl were immobilized on IFF-coated tubes at high cell density and found to exhibit higher luminescence intensities. Seawater medium cultures in the stationary phase were also effectively immobilized on IFF-coated tubes and emitted high luminescence. Specifically, IFF-immobilized V. fischeri cultures in seawater medium maintained their high luminescence emission for 30 days when stored at –70℃. In addition, a bioluminescence toxicity assay with various heavy metal solutions was carried out. Almost all the heavy metals tested decreased the luminescence of IFF-immobilized V. fischeri. However, the concentrations required for the effective attenuation of the luminescence were relatively high. In contrast, mercury (Hg(II)) rapidly dampened the luminescence intensity within a very narrow concentration range. Our findings on the emission of high-luminescence signals by IFF-immobilized V. fischeri provide a specific and efficient tool to detect low concentrations of Hg(II) compounds.